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Good morning everyone, and welcome to Day 3 of the training session for patients, consumers, and healthcare professionals involved in medicines regulatory activities. I am Michelle Belkin from the EMA's Scientific Evidence Generation Department, and I also coordinate our engagement with decision-makers, including HDA bodies. I'm thrilled to see around 60 registered participants, which reflects the widespread interest in this topic. As Maria mentioned, we've welcomed additional colleagues who are joining us for the first time, as this is the inaugural session for HDA Corporation activities.